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Rodney H Falk

Showing results (121-130 of 158) with videos related to

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European Journal of Heart Failure|April 30, 2021
Left atrial structure and function of the amyloidogenic V122I transthyretin variant in elderly African AmericansMasatoshi Minamisawa, Riccardo M Inciardi, Brian Claggett, et al.
JACC. Cardiovascular Imaging|December 15, 2023
Current and Evolving Multimodality Cardiac Imaging in Managing Transthyretin Amyloid CardiomyopathyLouhai Alwan, Dominik C Benz, Sarah A M Cuddy, et al.
JAMA Cardiology|March 17, 2019
Association of Patisiran, an RNA Interference Therapeutic, With Regional Left Ventricular Myocardial Strain in Hereditary Transthyretin Amyloidosis: The APOLLO StudyMasatoshi Minamisawa, Brian Claggett, David Adams, et al.
Annals of Internal Medicine|January 22, 2004
High-dose melphalan and autologous stem-cell transplantation in patients with AL amyloidosis: an 8-year studyMartha Skinner, Vaishali Sanchorawala, David C Seldin, et al.
JACC. Cardiovascular Imaging|August 20, 2018
Relative Apical Sparing of Myocardial Longitudinal Strain Is Explained by Regional Differences in Total Amyloid Mass Rather Than the Proportion of Amyloid DepositsPaco E Bravo, Kana Fujikura, Marie Foley Kijewski, et al.
Circulation. Cardiovascular Imaging|November 15, 2022
Optimal Echocardiographic Parameters to Improve the Diagnostic Yield of Tc-99m-Bone Avid Tracer Cardiac Scintigraphy for Transthyretin Cardiac AmyloidosisSarah Am Cuddy, Yesh Datar, Gavin Ovsak, et al.
Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine|April 8, 2019
Early Detection of Multiorgan Light-Chain Amyloidosis by Whole-Body <sup>18</sup>F-Florbetapir PET/CTEric C Ehman, M Samir El-Sady, Marie F Kijewski, et al.
JACC. Heart Failure|September 7, 2024
Functional Status and Quality of Life in Light-Chain Amyloidosis: Advanced Imaging, Longitudinal Changes, and OutcomesOlivier F Clerc, Shilpa Vijayakumar, Sarah A M Cuddy, et al.
Cardiovascular Drugs and Therapy|February 17, 2020
Phase 3 Multicenter Study of Revusiran in Patients with Hereditary Transthyretin-Mediated (hATTR) Amyloidosis with Cardiomyopathy (ENDEAVOUR)Daniel P Judge, Arnt V Kristen, Martha Grogan, et al.
Cardiovascular Drugs and Therapy|June 18, 2020
Correction to: Phase 3 Multicenter Study of Revusiran in Patients with Hereditary Transthyretin-Mediated (hATTR) Amyloidosis with Cardiomyopathy (ENDEAVOUR)Daniel P Judge, Arnt V Kristen, Martha Grogan, et al.
Pageof 16

Showing results (121-130 of 158) with videos related to

Sort By:
Pageof 16
European Journal of Heart Failure|April 30, 2021
Left atrial structure and function of the amyloidogenic V122I transthyretin variant in elderly African AmericansMasatoshi Minamisawa, Riccardo M Inciardi, Brian Claggett, et al.
JACC. Cardiovascular Imaging|December 15, 2023
Current and Evolving Multimodality Cardiac Imaging in Managing Transthyretin Amyloid CardiomyopathyLouhai Alwan, Dominik C Benz, Sarah A M Cuddy, et al.
JAMA Cardiology|March 17, 2019
Association of Patisiran, an RNA Interference Therapeutic, With Regional Left Ventricular Myocardial Strain in Hereditary Transthyretin Amyloidosis: The APOLLO StudyMasatoshi Minamisawa, Brian Claggett, David Adams, et al.
Annals of Internal Medicine|January 22, 2004
High-dose melphalan and autologous stem-cell transplantation in patients with AL amyloidosis: an 8-year studyMartha Skinner, Vaishali Sanchorawala, David C Seldin, et al.
JACC. Cardiovascular Imaging|August 20, 2018
Relative Apical Sparing of Myocardial Longitudinal Strain Is Explained by Regional Differences in Total Amyloid Mass Rather Than the Proportion of Amyloid DepositsPaco E Bravo, Kana Fujikura, Marie Foley Kijewski, et al.
Circulation. Cardiovascular Imaging|November 15, 2022
Optimal Echocardiographic Parameters to Improve the Diagnostic Yield of Tc-99m-Bone Avid Tracer Cardiac Scintigraphy for Transthyretin Cardiac AmyloidosisSarah Am Cuddy, Yesh Datar, Gavin Ovsak, et al.
Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine|April 8, 2019
Early Detection of Multiorgan Light-Chain Amyloidosis by Whole-Body <sup>18</sup>F-Florbetapir PET/CTEric C Ehman, M Samir El-Sady, Marie F Kijewski, et al.
JACC. Heart Failure|September 7, 2024
Functional Status and Quality of Life in Light-Chain Amyloidosis: Advanced Imaging, Longitudinal Changes, and OutcomesOlivier F Clerc, Shilpa Vijayakumar, Sarah A M Cuddy, et al.
Cardiovascular Drugs and Therapy|February 17, 2020
Phase 3 Multicenter Study of Revusiran in Patients with Hereditary Transthyretin-Mediated (hATTR) Amyloidosis with Cardiomyopathy (ENDEAVOUR)Daniel P Judge, Arnt V Kristen, Martha Grogan, et al.
Cardiovascular Drugs and Therapy|June 18, 2020
Correction to: Phase 3 Multicenter Study of Revusiran in Patients with Hereditary Transthyretin-Mediated (hATTR) Amyloidosis with Cardiomyopathy (ENDEAVOUR)Daniel P Judge, Arnt V Kristen, Martha Grogan, et al.
Pageof 16